Parexel - IT - Administration

Join Parexel as a Site Activation Partner in Ontario, Canada. Leverage your 2+ years of Study Start Up experience to manage essential documents and investigator site initiation. Ensure regulatory compliance with ICH/GCP and FDA guidelines while coordinating global clinical trials. Advance your ca...

We are seeking a Contracts Manager to join our global team, based in Dublin, London, or Belgrade. You will lead contract negotiations, manage client relationships, and oversee budgets for clinical trials. Ideal candidates possess a university degree, strong negotiation skills, and industry experi...

Lead global clinical trials for biotech clients in this remote US role. Utilize your project management expertise within a CRO or pharma setting to deliver patient-focused studies. Drive operational excellence while enjoying a supportive, flexible environment with diverse therapeutic challenges.

Lead cross-functional clinical trial teams in Bengaluru to deliver patient-focused studies and accelerate treatments to market. This role requires project management skills, a science degree, and strong English proficiency. Enjoy a supportive, flexible environment with diverse projects and clear ...

Join Parexel, a leading global CRO, as a Clinical Operations Assistant. Support CRAs and project teams with administrative tasks, site payments, and trial master file management in this remote Mexico role. Requires a healthcare/science degree, English fluency, and site experience. Contribute to l...

Lead the development of global processes and procedural documentation (SOPs, policies) for a major sponsor's clinical, medical, and safety organizations. This senior remote role in Argentina, Brazil, or Mexico requires 5-8 years of pharmaceutical process design experience. You will manage complex...

Lead our Site and Monitoring Health team, ensuring clinical trial quality and CRO oversight. This site-facing role requires significant monitoring and lead CRA experience, with up to 50% travel. Apply your expertise in GCP, risk-based oversight, and innovative problem-solving within a US-based FS...

Lead global clinical trials as a Senior Manager in this fully remote role based in Italy or the UK. You will provide end-to-end operational leadership, ensuring on-time and compliant delivery. Essential requirements include 7+ years of global trial management and CRO oversight experience. Drive s...

Join our team as a Central Monitor in Romania. You will ensure clinical trial data quality and oversight using risk-based monitoring and data analytics. The role requires 5+ years of pharma/CRO experience and expertise in RBQM and central monitoring. You'll play a key role in risk identification ...

Join our team in Serbia as a Central Monitor (FSP). You will ensure clinical trial data quality and oversight using risk-based monitoring and data analytics. The role requires ≥5 years of pharma/CRO experience and expertise in central monitoring and RBQM. You'll play a key role in risk identifica...